GUDIDData
eudamed_udi Primary ID: D-EBX-020-09BE

EurobioPlex Méningite bactérienne communautaire (UDI D-EBX-020-09BE)

Manufactured by Eurobio Scientific

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EurobioPlex Méningite bactérienne communautaire - Primary ID D-EBX-020-09BE

Device Regulatory Overview

The EurobioPlex Méningite bactérienne communautaire (Model/Catalog Number: EBX-020-09) is a medical device manufactured by Eurobio Scientific. This product is indexed under FDA Product Code / Category Classification W0105070505 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EBX-020-09
Product Code / EMDN
W0105070505
Device Name
EurobioPlex Méningite bactérienne communautaire
Database Sync Date
2026-08-09 16:29:36

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of EurobioPlex Méningite bactérienne communautaire?

The registered manufacturer of record for EurobioPlex Méningite bactérienne communautaire is Eurobio Scientific.

What is the Primary UDI-DI identifier for EurobioPlex Méningite bactérienne communautaire?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-EBX-020-09BE.

What classification code is assigned to this device?

This device is registered under product classification code W0105070505.

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